A citation-based method for searching scientific literature

Elisa Balzano, Franca Pelliccia, Simona Giunta. Semin Cell Dev Biol 2021
Times Cited: 1







List of co-cited articles
articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


The pathogenic exon 1 HTT protein is produced by incomplete splicing in Huntington's disease patients.
Andreas Neueder, Christian Landles, Rhia Ghosh, David Howland, Richard H Myers, Richard L M Faull, Sarah J Tabrizi, Gillian P Bates. Sci Rep 2017
63
100

Mutant CAG repeats of Huntingtin transcript fold into hairpins, form nuclear foci and are targets for RNA interference.
Mateusz de Mezer, Marzena Wojciechowska, Marek Napierala, Krzysztof Sobczak, Wlodzimierz J Krzyzosiak. Nucleic Acids Res 2011
115
100

Poly(GR) impairs protein translation and stress granule dynamics in C9orf72-associated frontotemporal dementia and amyotrophic lateral sclerosis.
Yong-Jie Zhang, Tania F Gendron, Mark T W Ebbert, Aliesha D O'Raw, Mei Yue, Karen Jansen-West, Xu Zhang, Mercedes Prudencio, Jeannie Chew, Casey N Cook,[...]. Nat Med 2018
112
100

Somatic instability of CTG repeat in myotonic dystrophy.
T Ashizawa, J R Dubel, Y Harati. Neurology 1993
148
100

Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n.
E J Kremer, M Pritchard, M Lynch, S Yu, K Holman, E Baker, S T Warren, D Schlessinger, G R Sutherland, R I Richards. Science 1991
800
100

A Māori specific RFC1 pathogenic repeat configuration in CANVAS, likely due to a founder allele.
Sarah J Beecroft, Andrea Cortese, Roisin Sullivan, Wai Yan Yau, Zoe Dyer, Teddy Y Wu, Eoin Mulroy, Luciana Pelosi, Miriam Rodrigues, Rachael Taylor,[...]. Brain 2020
6
100

Bioinformatics-Based Identification of Expanded Repeats: A Non-reference Intronic Pentamer Expansion in RFC1 Causes CANVAS.
Haloom Rafehi, David J Szmulewicz, Mark F Bennett, Nara L M Sobreira, Kate Pope, Katherine R Smith, Greta Gillies, Peter Diakumis, Egor Dolzhenko, Michael A Eberle,[...]. Am J Hum Genet 2019
53
100

CUG initiation and frameshifting enable production of dipeptide repeat proteins from ALS/FTD C9ORF72 transcripts.
Ricardos Tabet, Laure Schaeffer, Fernande Freyermuth, Melanie Jambeau, Michael Workman, Chao-Zong Lee, Chun-Chia Lin, Jie Jiang, Karen Jansen-West, Hussein Abou-Hamdan,[...]. Nat Commun 2018
60
100

Chimeric Peptide Species Contribute to Divergent Dipeptide Repeat Pathology in c9ALS/FTD and SCA36.
Zachary T McEachin, Tania F Gendron, Nisha Raj, María García-Murias, Anwesha Banerjee, Ryan H Purcell, Patricia J Ward, Tiffany W Todd, Megan E Merritt-Garza, Karen Jansen-West,[...]. Neuron 2020
14
100

DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseases.
Conceição Bettencourt, Davina Hensman-Moss, Michael Flower, Sarah Wiethoff, Alexis Brice, Cyril Goizet, Giovanni Stevanin, Georgios Koutsis, Georgia Karadima, Marios Panas,[...]. Ann Neurol 2016
107
100

Testosterone reduction prevents phenotypic expression in a transgenic mouse model of spinal and bulbar muscular atrophy.
Masahisa Katsuno, Hiroaki Adachi, Akito Kume, Mei Li, Yuji Nakagomi, Hisayoshi Niwa, Chen Sang, Yasushi Kobayashi, Manabu Doyu, Gen Sobue. Neuron 2002
346
100


RNA Droplets.
Kevin Rhine, Velinda Vidaurre, Sua Myong. Annu Rev Biophys 2020
23
100

Differential Toxicity of Nuclear RNA Foci versus Dipeptide Repeat Proteins in a Drosophila Model of C9ORF72 FTD/ALS.
Helene Tran, Sandra Almeida, Jill Moore, Tania F Gendron, UmaDevi Chalasani, Yubing Lu, Xing Du, Jeffrey A Nickerson, Leonard Petrucelli, Zhiping Weng,[...]. Neuron 2015
127
100

Translation of GGC repeat expansions into a toxic polyglycine protein in NIID defines a novel class of human genetic disorders: The polyG diseases.
Manon Boivin, Jianwen Deng, Véronique Pfister, Erwan Grandgirard, Mustapha Oulad-Abdelghani, Bastien Morlet, Frank Ruffenach, Luc Negroni, Pascale Koebel, Hugues Jacob,[...]. Neuron 2021
3
100

Hexanucleotide repeats in ALS/FTD form length-dependent RNA foci, sequester RNA binding proteins, and are neurotoxic.
Youn-Bok Lee, Han-Jou Chen, João N Peres, Jorge Gomez-Deza, Jan Attig, Maja Stalekar, Claire Troakes, Agnes L Nishimura, Emma L Scotter, Caroline Vance,[...]. Cell Rep 2013
290
100

Lack of a Clear Behavioral Phenotype in an Inducible FXTAS Mouse Model Despite the Presence of Neuronal FMRpolyG-Positive Aggregates.
Saif N Haify, Ruchira S D Mankoe, Valerie Boumeester, Esmay C van der Toorn, Rob F M Verhagen, Rob Willemsen, Renate K Hukema, Laurens W J Bosman. Front Mol Biosci 2020
1
100

Promoter-bound trinucleotide repeat mRNA drives epigenetic silencing in fragile X syndrome.
Dilek Colak, Nikica Zaninovic, Michael S Cohen, Zev Rosenwaks, Wang-Yong Yang, Jeannine Gerhardt, Matthew D Disney, Samie R Jaffrey. Science 2014
179
100

Finding and extending ancient simple sequence repeat-derived regions in the human genome.
Jonathan A Shortt, Robert P Ruggiero, Corey Cox, Aaron C Wacholder, David D Pollock. Mob DNA 2020
4
100

On the wrong DNA track: Molecular mechanisms of repeat-mediated genome instability.
Alexandra N Khristich, Sergei M Mirkin. J Biol Chem 2020
30
100

Heterochromatin anomalies and double-stranded RNA accumulation underlie C9orf72 poly(PR) toxicity.
Yong-Jie Zhang, Lin Guo, Patrick K Gonzales, Tania F Gendron, Yanwei Wu, Karen Jansen-West, Aliesha D O'Raw, Sarah R Pickles, Mercedes Prudencio, Yari Carlomagno,[...]. Science 2019
77
100

Ribosomal frameshifting on MJD-1 transcripts with long CAG tracts.
André Toulouse, Faith Au-Yeung, Claudia Gaspar, Julie Roussel, Patrick Dion, Guy A Rouleau. Hum Mol Genet 2005
42
100

Glycine-alanine dipeptide repeat protein contributes to toxicity in a zebrafish model of C9orf72 associated neurodegeneration.
Yu Ohki, Andrea Wenninger-Weinzierl, Alexander Hruscha, Kazuhide Asakawa, Koichi Kawakami, Christian Haass, Dieter Edbauer, Bettina Schmid. Mol Neurodegener 2017
36
100

Foci of trinucleotide repeat transcripts in nuclei of myotonic dystrophy cells and tissues.
K L Taneja, M McCurrach, M Schalling, D Housman, R H Singer. J Cell Biol 1995
447
100

Metformin inhibits RAN translation through PKR pathway and mitigates disease in C9orf72 ALS/FTD mice.
Tao Zu, Shu Guo, Olgert Bardhi, Daniel A Ryskamp, Jian Li, Solaleh Khoramian Tusi, Avery Engelbrecht, Kelena Klippel, Paramita Chakrabarty, Lien Nguyen,[...]. Proc Natl Acad Sci U S A 2020
11
100

hnRNP A3 binds to GGGGCC repeats and is a constituent of p62-positive/TDP43-negative inclusions in the hippocampus of patients with C9orf72 mutations.
Kohji Mori, Sven Lammich, Ian R A Mackenzie, Ignasi Forné, Sonja Zilow, Hans Kretzschmar, Dieter Edbauer, Jonathan Janssens, Gernot Kleinberger, Marc Cruts,[...]. Acta Neuropathol 2013
220
100

Patterns of de novo tandem repeat mutations and their role in autism.
Ileena Mitra, Bonnie Huang, Nima Mousavi, Nichole Ma, Michael Lamkin, Richard Yanicky, Sharona Shleizer-Burko, Kirk E Lohmueller, Melissa Gymrek. Nature 2021
9
100

Arginine-rich dipeptide-repeat proteins as phase disruptors in C9-ALS/FTD.
Hana M Odeh, James Shorter. Emerg Top Life Sci 2020
8
100

Disruption of RNA Metabolism in Neurological Diseases and Emerging Therapeutic Interventions.
Julia K Nussbacher, Ricardos Tabet, Gene W Yeo, Clotilde Lagier-Tourenne. Neuron 2019
67
100


Drosophila screen connects nuclear transport genes to DPR pathology in c9ALS/FTD.
Steven Boeynaems, Elke Bogaert, Emiel Michiels, Ilse Gijselinck, Anne Sieben, Ana Jovičić, Greet De Baets, Wendy Scheveneels, Jolien Steyaert, Ivy Cuijt,[...]. Sci Rep 2016
150
100

Targeting CAG repeat RNAs reduces Huntington's disease phenotype independently of huntingtin levels.
Laura Rué, Mónica Bañez-Coronel, Jordi Creus-Muncunill, Albert Giralt, Rafael Alcalá-Vida, Gartze Mentxaka, Birgit Kagerbauer, M Teresa Zomeño-Abellán, Zeus Aranda, Veronica Venturi,[...]. J Clin Invest 2016
40
100

ATXN1 intermediate-length polyglutamine expansions are associated with amyotrophic lateral sclerosis.
Serena Lattante, Maria Grazia Pomponi, Amelia Conte, Giuseppe Marangi, Giulia Bisogni, Agata Katia Patanella, Emiliana Meleo, Christian Lunetta, Nilo Riva, Lorena Mosca,[...]. Neurobiol Aging 2018
22
100


Initial sequencing and analysis of the human genome.
E S Lander, L M Linton, B Birren, C Nusbaum, M C Zody, J Baldwin, K Devon, K Dewar, M Doyle, W FitzHugh,[...]. Nature 2001
100

NIPA1 polyalanine repeat expansions are associated with amyotrophic lateral sclerosis.
Hylke M Blauw, Wouter van Rheenen, Max Koppers, Philip Van Damme, Stefan Waibel, Robin Lemmens, Paul W J van Vught, Thomas Meyer, Claudia Schulte, Thomas Gasser,[...]. Hum Mol Genet 2012
32
100

CGG Repeat-Associated Non-AUG Translation Utilizes a Cap-Dependent Scanning Mechanism of Initiation to Produce Toxic Proteins.
Michael G Kearse, Katelyn M Green, Amy Krans, Caitlin M Rodriguez, Alexander E Linsalata, Aaron C Goldstrohm, Peter K Todd. Mol Cell 2016
77
100


Developmental study of fragile X syndrome using human embryonic stem cells derived from preimplantation genetically diagnosed embryos.
Rachel Eiges, Achia Urbach, Mira Malcov, Tsvia Frumkin, Tamar Schwartz, Ami Amit, Yuval Yaron, Amir Eden, Ofra Yanuka, Nissim Benvenisty,[...]. Cell Stem Cell 2007
200
100

FAST-1 antisense RNA epigenetically alters FXN expression.
Hajar Mikaeili, Madhavi Sandi, Aurélien Bayot, Sahar Al-Mahdawi, Mark A Pook. Sci Rep 2018
5
100

The CTG repeat expansion size correlates with the splicing defects observed in muscles from myotonic dystrophy type 1 patients.
A Botta, F Rinaldi, C Catalli, L Vergani, E Bonifazi, V Romeo, E Loro, A Viola, C Angelini, G Novelli. J Med Genet 2008
36
100

GGGGCC microsatellite RNA is neuritically localized, induces branching defects, and perturbs transport granule function.
Alondra Schweizer Burguete, Sandra Almeida, Fen-Biao Gao, Robert Kalb, Michael R Akins, Nancy M Bonini. Elife 2015
58
100

Antisense proline-arginine RAN dipeptides linked to C9ORF72-ALS/FTD form toxic nuclear aggregates that initiate in vitro and in vivo neuronal death.
Xinmei Wen, Wenzhi Tan, Thomas Westergard, Karthik Krishnamurthy, Shashirekha S Markandaiah, Yingxiao Shi, Shaoyu Lin, Neil A Shneider, John Monaghan, Udai B Pandey,[...]. Neuron 2014
281
100

RNA-binding proteins hnRNP A2/B1 and CUGBP1 suppress fragile X CGG premutation repeat-induced neurodegeneration in a Drosophila model of FXTAS.
Oyinkan A Sofola, Peng Jin, Yunlong Qin, Ranhui Duan, Huijie Liu, Maria de Haro, David L Nelson, Juan Botas. Neuron 2007
233
100

Antisense transcripts of the expanded C9ORF72 hexanucleotide repeat form nuclear RNA foci and undergo repeat-associated non-ATG translation in c9FTD/ALS.
Tania F Gendron, Kevin F Bieniek, Yong-Jie Zhang, Karen Jansen-West, Peter E A Ash, Thomas Caulfield, Lillian Daughrity, Judith H Dunmore, Monica Castanedes-Casey, Jeannie Chew,[...]. Acta Neuropathol 2013
333
100

Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2.
C Jones, L Penny, T Mattina, S Yu, E Baker, L Voullaire, W Y Langdon, G R Sutherland, R I Richards, A Tunnacliffe. Nature 1995
159
100

In Situ Architecture and Cellular Interactions of PolyQ Inclusions.
Felix J B Bäuerlein, Itika Saha, Archana Mishra, Maria Kalemanov, Antonio Martínez-Sánchez, Rüdiger Klein, Irina Dudanova, Mark S Hipp, F Ulrich Hartl, Wolfgang Baumeister,[...]. Cell 2017
120
100

Cellular toxicity of expanded RNA repeats: focus on RNA foci.
Marzena Wojciechowska, Wlodzimierz J Krzyzosiak. Hum Mol Genet 2011
153
100

eIF4B and eIF4H mediate GR production from expanded G4C2 in a Drosophila model for C9orf72-associated ALS.
Lindsey D Goodman, Mercedes Prudencio, Ananth R Srinivasan, Olivia M Rifai, Virginia M-Y Lee, Leonard Petrucelli, Nancy M Bonini. Acta Neuropathol Commun 2019
17
100

Expanded CUG repeat RNAs form hairpins that activate the double-stranded RNA-dependent protein kinase PKR.
B Tian, R J White, T Xia, S Welle, D H Turner, M B Mathews, C A Thornton. RNA 2000
171
100


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.